A unifying aetiological explanation for anomalies of human tooth number and size.

Genetic and environmental factors are implicated in the aetiology of supernumerary teeth, hypodontia, megadontia and microdontia ; these anomalies tend to be associated. 1115 school children aged 11-14 years examined clinically and radiographically provided prevalence data. A further 703 children with dental anomalies were studied. 153 of these became probands for a family study and 327 of their first-degree relatives were examined. There were much higher frequencies (p less than 0.001) of all anomalies among the relatives of probands than in the general population. Males more often had supernumerary teeth and megadontia and females more frequently had hypodontia (p less than 0.05) and microdontia . For hypodontia, the proportion of relatives affected varied with the severity of the condition in the proband (p less than 0.05). In the prevalence study, there was an association between hypodontia and microdontia (p less than 0.001). These findings may be explained by a multifactorial model having a continuous scale, related to tooth number and size, with thresholds. Position on the scale usually depends upon the combination of numerous genetic and environmental factors, each with a small effect, but occasionally a chromosomal anomaly, a major single gene or a major environmental insult may have a large effect. The finding that the estimated difference between the means of the sexes was the same for each anomaly, within the limits of experimental error, supports the validity of the model.

[1]  B. Baum,et al.  Studies on agenesis in the permanent dentition. , 1971, American journal of physical anthropology.

[2]  Woolf Cm Missing maxillary lateral incisors: a genetic study. , 1971 .

[3]  A. Rantanen On the frequency of the missing and pegshaped maxillary lateral incisor among Finnish students. , 1956, American journal of physical anthropology.

[4]  A. Miles,et al.  Malformations of the Teeth , 1954, Proceedings of the Royal Society of Medicine.

[5]  N. Myrberg,et al.  Mesiodistal tooth size in the deciduous and permanent dentitions. , 1982, European journal of orthodontics.

[6]  Johnson Db,et al.  Variation in the expression of hypodontia in monozygotic twins. , 1971 .

[7]  C. Moorrees,et al.  Mesiodistal Crown Diameters of the Deciduous and Permanent Teeth in Individuals , 1957, Journal of dental research.

[8]  Bailit Hl,et al.  Dental variation among populations. An anthropologic view. , 1975 .

[9]  C. Chung,et al.  Developmental interaction, size and agenesis among permanent maxillary incisors. , 1971, Human biology.

[10]  G. B. Winter,et al.  Oral manifestations of chondroectodermal dysplasia (Ellis-Van Creveld Syndrome). Report of a case. , 1967, British dental journal.

[11]  M. Simpkiss,et al.  Hypertrichosis with hereditary gingival hyperplasia , 1974, Archives of disease in childhood.

[12]  H. Grüneberg The genetics of a tooth defect in the mouse , 1951, Proceedings of the Royal Society of London. Series B - Biological Sciences.

[13]  Winter Gb,et al.  Autosomal dominant ectodermal dysplasia with significant dental defects. , 1969 .

[14]  J. Sofaer,et al.  Aspects of the tabby-crinkled-downless syndrome. I. The development of tabby teeth. , 1969, Journal of embryology and experimental morphology.

[15]  M. Rushton Effects of radium on the dentition. , 1947, American journal of orthodontics.

[16]  K. Bergström An orthopantomographic study of hypodontia, supernumeraries and other anomalies in school children between the ages of 8-9 years. An epidemiological study. , 1977, Swedish dental journal.

[17]  V. Alexandersen,et al.  Macrodontic maxillary second primary molar in an Eskimo skull. An morphogenetic study. , 1970, Scandinavian journal of dental research.

[18]  K. Hellgren,et al.  Children with Thalidomide Emrryopathy: Odontological Observations and Aspects , 1966 .

[19]  C. Carter Genetics of common disorders. , 1969, British medical bulletin.

[20]  L. Alvesalo,et al.  The inheritance pattern of missing, peg-shaped, and strongly mesio-distally reduced upper lateral incisors. , 1969, Acta odontologica Scandinavica.

[21]  S. Garn,et al.  Third Molar Agenesis and Size Reduction of the Remaining Teeth , 1963, Nature.

[22]  L. Mandeville Congenital absence of permanent maxillary lateral incisor teeth; a preliminary investigation. , 1949, Annals of eugenics.

[23]  Lavelle Cl Comparison of the deciduous teeth between Caucasoid, Negroid, and Mongoloid population samples. , 1970 .

[24]  G. Townsend Heritability of deciduous tooth size in Australian aboriginals. , 1980, American journal of physical anthropology.

[25]  S. Steigman,et al.  Relationship between mesiodistal crown diameter of posterior deciduous and succedaneous teeth in israeli children. , 1982, European journal of orthodontics.

[26]  G. Townsend,et al.  Heritability of permanent tooth size. , 1978, American journal of physical anthropology.

[27]  J. D. Niswander,et al.  CONGENITAL ANOMALIES OF TEETH IN JAPANESE CHILDREN. , 1963, American journal of physical anthropology.

[28]  E. H. Ashton,et al.  Cusp pattern, tooth size and third molar agenesis in the human mandibular dentition. , 1970, Archives of oral biology.

[29]  M. Grewal The Development of an Inherited Tooth Defect in the Mouse , 1962 .

[30]  S. Ø. Thomsen Missing teeth with special reference to the population of Tristan da Cunha. , 1952, American journal of physical anthropology.

[31]  Gullikson Js Tooth morphology in rubella syndrome children. , 1975 .

[32]  B. Baum,et al.  Agenesis and tooth size in the permanent dentition. , 1971, The Angle orthodontist.

[33]  T. Cohen,et al.  Hypodontia: A Polygenic Trait-A Family Study among Israeli Jews , 1975, Journal of dental research.